Stajich JM - Search Results

1

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Among authors: stajich jm. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

2

Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.

Speer MC, Graham FL, Bonner E, Collier K, Stajich JM, Gaskell PC, Pericak-Vance MA, Vance JM. Speer MC, et al. Among authors: stajich jm. Neurogenetics. 2002 Oct;4(2):83-5. doi: 10.1007/s10048-002-0139-3. Neurogenetics. 2002. PMID: 12481986

3

A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17.

Lucas AM, Vance JM, Stajich JM, Roses AD. Lucas AM, et al. Among authors: stajich jm. Nucleic Acids Res. 1991 Oct 25;19(20):5802. doi: 10.1093/nar/19.20.5802-a. Nucleic Acids Res. 1991. PMID: 1682890 Free PMC article. No abstract available.

4

Confirmation of linkage in von Hippel-Lindau disease.

Vance JM, Small KW, Jones MA, Stajich JM, Yamaoka LH, Roses AD, Hung WY, Pericak-Vance MA. Vance JM, et al. Among authors: stajich jm. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994

5

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al. Ben Othmane K, et al. Among authors: stajich jm. Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334. Genomics. 1993. PMID: 8406488

6

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Among authors: stajich j. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

7

Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.

Yamaoka LH, Pericak-Vance MA, Speer MC, Gaskell PC Jr, Stajich J, Haynes C, Hung WY, Laberge C, Thibault MC, Mathieu J, et al. Yamaoka LH, et al. Neurology. 1990 Feb;40(2):222-6. doi: 10.1212/wnl.40.2.222. Neurology. 1990. PMID: 2300239

8

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.

Vance JM, Nicholson GA, Yamaoka LH, Stajich J, Stewart CS, Speer MC, Hung WY, Roses AD, Barker D, Pericak-Vance MA. Vance JM, et al. Among authors: stajich j. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366

9

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS, et al. Speer MC, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Jun;50(6):1211-7. Am J Hum Genet. 1992. PMID: 1598902 Free PMC article.

10

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

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